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von Hippelova-Lindauova choroba
Č. záznamu d006623 Dátum 06.06.2025 Typ M Tematický termín von Hippelova-Lindauova choroba Iný termín Angličtina (Pseudonym) Cerebelloretinal Angiomatosis, Familial
Angličtina (Pseudonym) Lindau Disease
Slovenčina (Pseudonym) angiomatóza cerebeloretinálna familiárna
Slovenčina (Pseudonym) Lindauova choroba
Slovenčina (Pseudonym) Hippelova-Lindauova choroba
Slovenčina (Pseudonym) Hippel-Lindauova choroba
Slovenčina (Pseudonym) angiomatosis retinae
Slovenčina (Pseudonym) angiomatosis retinocerebellosa
Slovenčina (Pseudonym) von Hippelov-Lindauov syndróm
Slovenčina (Pseudonym) VHL syndróm
MDT C10.562.925C14.907.077.925C16.131.077.245.750C16.320.184.750 Poznámka An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. 
predmetové heslo
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